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Lipoxygenase and Cyclooxygenase Pathways and Colorectal Cancer Prevention

机译:脂氧合酶和环氧化酶途径和结直肠癌预防

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摘要

Colorectal cancer is one of the commonest malignancies in both men and women. In spite of significant progress in screening and in surgical and therapeutic interventions, colorectal cancer (CRC) is still a major public health problem. Accumulating evidence suggests that targeting inflammatory pathways may provide protection against the development of CRC. Eicosanoids derived from the enzymes cyclooxygenase (COX) and lipoxygenase (LOX) may contribute to CRC carcinogenesis. Approaches for targeting COX-1 and COX-2 with traditional nonsteroidal anti-inflammatory agents or targeting COX-2 with specific inhibitors are highly successful at the preclinical and clinical levels; however, large-scale clinical applicability of these agents is limited owing to unwanted side effects. Emerging studies suggests that 5-LOX-derived leukotrienes may contribute to colon tumor development and risk of thrombotic events. Thus, developing drugs that target both 5-LOX and COX-2 may provide a safer strategy. In this review, we discuss evidence for the involvement of 5-LOX in colon tumor development and targeting 5-LOX and COX-2 with synthetic and naturally occurring agents for CRC prevention.
机译:结直肠癌是男女中最常见的恶性肿瘤之一。尽管在筛查以及手术和治疗干预方面取得了重大进展,但结直肠癌(CRC)仍然是一个主要的公共卫生问题。越来越多的证据表明,靶向炎症途径可能提供针对CRC发生的保护作用。来源于环氧合酶(COX)和脂氧合酶(LOX)的类花生酸可能导致CRC致癌。在临床前和临床上,用传统的非甾体类抗炎药靶向COX-1和COX-2或用特异性抑制剂靶向COX-2的方法非常成功。然而,由于不希望的副作用,这些试剂的大规模临床应用受到限制。新兴研究表明,5-LOX衍生的白三烯可能有助于结肠肿瘤的发展和血栓形成事件的风险。因此,开发同时针对5-LOX和COX-2的药物可能会提供更安全的策略。在这篇综述中,我们讨论5-LOX参与结肠肿瘤发展并以合成和天然存在的CRC预防剂靶向5-LOX和COX-2的证据。

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